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  2. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    In organic chemistry, a cycloalkene or cycloolefin is a type of alkene hydrocarbon which contains a closed ring of carbon atoms and either one or more double bonds, but has no aromatic character. Some cycloalkenes, such as cyclobutene and cyclopentene , can be used as monomers to produce polymer chains. [ 1 ]

  3. Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctene

    Cyclooctene is the cycloalkene with a formula C 8 H 14. Its molecule has a ring of 8 carbon atoms, connected by seven single bonds and one double bond. Cyclooctene is notable because it is the smallest cycloalkene that can exist stably as either the cis or trans stereoisomer, with cis-cyclooctene being the most common.

  4. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The International Union of Pure and Applied Chemistry (IUPAC) recommends using the name "alkene" only for acyclic hydrocarbons with just one double bond; alkadiene, alkatriene, etc., or polyene for acyclic hydrocarbons with two or more double bonds; cycloalkene, cycloalkadiene, etc. for cyclic ones; and "olefin" for the general class – cyclic ...

  5. Cyclodecene - Wikipedia

    en.wikipedia.org/wiki/Cyclodecene

    Cyclodecene is a cycloalkene with a ten-membered ring, with two possible geometric isomers, denoted cis-cyclodecene and trans-cyclodecene, or (Z)-cyclodecene and (E)-cyclodecene. References [ edit ]

  6. trans-Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Trans-Cyclooctene

    trans-Cyclooctene was first synthesized on a preparatory scale by Arthur C. Cope with a Hofmann elimination reaction of N,N,N-trimethylcyclooctylammonium iodide. [10] The reaction gives a mixture of cis and trans isomers, and the trans isomer is selectively trapped as a complex with silver nitrate.

  7. Perfluorocycloalkene - Wikipedia

    en.wikipedia.org/wiki/Perfluorocycloalkene

    A perfluorocycloalkene (PFCA) fluorocarbon structure with a cycloalkene core. PFCAs have shown reactivity with a wide variety of nucleophiles including phenoxides, alkoxides, organometallic, amines, thiols, and azoles. [1]

  8. Cycloheptene - Wikipedia

    en.wikipedia.org/wiki/Cycloheptene

    One procedure for the organic synthesis of trans-cycloheptene is by singlet photosensitization of cis-cycloheptene with methyl benzoate and ultraviolet light at −35 °C. [2] The double bond in the trans isomer is very strained. [3] The directly attached atoms on a simple alkene are all coplanar.

  9. Cycloalkyne - Wikipedia

    en.wikipedia.org/wiki/Cycloalkyne

    A cycloalkyne consists of a closed ring of carbon atoms containing one or more triple bonds. Cycloalkynes have a general formula C n H 2 n −4 . Because of the linear nature of the C−C≡C−C alkyne unit, cycloalkynes can be highly strained and can only exist when the number of carbon atoms in the ring is great enough to provide the ...